Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03721250
Other study ID # Ank230918
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 14, 2018
Est. completion date April 22, 2019

Study information

Verified date February 2020
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Postoperative pain is an important issue after thoracotomy operations. Thoracic epidural analgesia is most popular analgesic method, but sometimes it is not sufficient for pain. This study is designed to compare intercostal block with thoracic epidural analgesia in patients undergoing thoracotomy


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 22, 2019
Est. primary completion date March 4, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

lung cancer

Exclusion Criteria:

patient refusal bleeding diathesisi emergency cases

-

Study Design


Related Conditions & MeSH terms


Intervention

Other:
epidural
thoracic epidural analgesia

Locations

Country Name City State
Turkey Ankara University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary verbal analog score postoperative 24 hour
See also
  Status Clinical Trial Phase
Completed NCT00800826 - The Combination Effect of Dexmedetomidine and Morphine in Postoperative Patient-Controlled Analgesia Phase 4
Completed NCT03541941 - Exparel vs. Bupivacaine Hydrochloride vs. Placebo for Hernia Repair Phase 4
Withdrawn NCT03143530 - Effect of Pectoralis Block on Analgesia After Simple Mastectomy Phase 4